Surgidyne Varidyne, Model 140-2I & Model 140-2ID

FDA 510(k) K860030 · Surgidyne, Inc.

Substantially Equivalent

510(k) numberK860030

Submission

Device name
Surgidyne Varidyne, Model 140-2I & Model 140-2ID
Applicant
Surgidyne, Inc.
Eden Prairie, MN, US
Received
January 6, 1986
Decision date
February 12, 1986
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
BTA – Pump, Portable, Aspiration (Manual Or Powered)
Device class
Class II (moderate risk)
Regulation
21 CFR 878.4780
Specialty
General, Plastic Surgery

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More from Shenzhen Kingboom Technology Co., Ltd.

510(k)DeviceDecision
K892334Leonard TubeKDH · Traditional 05/31/1989SE
K883582Varidyne Model 250 Suction Drainage SystemBTA · Traditional 10/03/1988SE
K864822Varidyne 550, Models 12E,12M,24E & 24M Suction SysBTC · Traditional 01/15/1987SE
K852180Surgidynes Varidyne 350-2I & 350-2C Cordless Elec. · Traditional 07/01/1985SN
K850634Surgidyne Surgiflo C.W.S. Drain ProductsGCY · Traditional 06/28/1985SE

Questions and answers

When was Surgidyne Varidyne, Model 140-2I & Model 140-2ID cleared by the FDA?

Surgidyne Varidyne, Model 140-2I & Model 140-2ID (K860030) received a 510(k) decision of Substantially Equivalent on February 12, 1986, 37 days after the submission was received.

What is the product code of K860030?

The FDA product code is BTA – Pump, Portable, Aspiration (Manual Or Powered), a Class II (moderate risk) device regulated under 21 CFR 878.4780.